Institute of Molecular Physiology and Genetics, Center of Biosciences, Slovak Academy of Sciences, Dúbravská Cesta 9, 840 05 Bratislava, Slovakia.
Int J Mol Sci. 2020 Dec 15;21(24):9532. doi: 10.3390/ijms21249532.
Atypical antipsychotic drugs were introduced in the early 1990s. Unlike typical antipsychotics, which are effective only against positive symptoms of schizophrenia, atypical antipsychotics are effective against negative and cognitive symptoms as well. Furthermore, they are effective not only in psychotic but also in affective disorders, on their own or as adjuncts to antidepressant drugs. This review presents the neural mechanisms of currently existing atypical antipsychotics and putative antipsychotics currently being investigated in preclinical and clinical studies and how these relate to their effectiveness in mood disorders such as depression, anxiety, and post-traumatic stress disorder (PTSD). Typical antipsychotics act almost exclusively on the dopamine system. Atypical drugs, however, modulate serotonin (5-HT), norepinephrine, and/or histamine neurotransmission as well. This multimodal mechanism of action putatively underlies the beneficial effect of atypical antipsychotics in mood and anxiety disorders. Interestingly, novel experimental drugs having dual antipsychotic and antidepressant therapeutic potential, such as histamine, adenosine, and trace amine-associated receptors (TAAR) ligand, are also characterized by a multimodal stimulatory effect on central 5-HT, norepinephrine, and/or histamine transmission. The multimodal stimulatory effect on central monoamine neurotransmission may be thus primarily responsible for the combined antidepressant and antipsychotic therapeutic potential of certain central nervous system (CNS) drugs.
非典型抗精神病药物于 20 世纪 90 年代初问世。与仅对精神分裂症阳性症状有效的典型抗精神病药物不同,非典型抗精神病药物对阴性症状和认知症状也有效。此外,它们不仅对精神病有效,而且对情感障碍也有效,无论是单独使用还是作为抗抑郁药物的辅助药物。本综述介绍了目前存在的非典型抗精神病药物和目前在临床前和临床研究中研究的假定抗精神病药物的神经机制,以及这些机制如何与其在抑郁症、焦虑症和创伤后应激障碍(PTSD)等情绪障碍中的疗效相关。典型抗精神病药物几乎只作用于多巴胺系统。然而,非典型药物也调节 5-羟色胺(5-HT)、去甲肾上腺素和/或组胺神经传递。这种多模态作用机制推测是非典型抗精神病药物在情绪和焦虑障碍中有益作用的基础。有趣的是,具有双重抗精神病和抗抑郁治疗潜力的新型实验药物,如组胺、腺苷和微量胺相关受体(TAAR)配体,也表现出对中枢 5-HT、去甲肾上腺素和/或组胺传递的多模态刺激作用。因此,中枢单胺神经递质的多模态刺激作用可能是某些中枢神经系统(CNS)药物具有抗抑郁和抗精神病联合治疗潜力的主要原因。